Product NDC: | 47219-200 |
Proprietary Name: | Nyloxin |
Non Proprietary Name: | NAJA NAJA VENOM |
Active Ingredient(s): | 4 [hp_X]/mL & nbsp; NAJA NAJA VENOM |
Administration Route(s): | ORAL |
Dosage Form(s): | SPRAY, METERED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 47219-200 |
Labeler Name: | Receptopharm Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20100823 |
Package NDC: | 47219-200-01 |
Package Description: | 1 BOTTLE, SPRAY in 1 BOX (47219-200-01) > 30 mL in 1 BOTTLE, SPRAY |
NDC Code | 47219-200-01 |
Proprietary Name | Nyloxin |
Package Description | 1 BOTTLE, SPRAY in 1 BOX (47219-200-01) > 30 mL in 1 BOTTLE, SPRAY |
Product NDC | 47219-200 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | NAJA NAJA VENOM |
Dosage Form Name | SPRAY, METERED |
Route Name | ORAL |
Start Marketing Date | 20100823 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Receptopharm Inc. |
Substance Name | NAJA NAJA VENOM |
Strength Number | 4 |
Strength Unit | [hp_X]/mL |
Pharmaceutical Classes |